Canonical Allele Identifier: CA2574561400

Gene: SIRT1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.67908186T>A , CM000672.2:g.67908186T>A	GRCh38
NC_000010.10:g.69667943T>A , CM000672.1:g.69667943T>A	GRCh37
NC_000010.9:g.69337949T>A	NCBI36
NG_050664.1:g.28525T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000212015.11:c.1170+61T>A MANE Select	ENSP00000212015.6:n.1170+61T>A
ENST00000212015.10:c.1170+61T>A	ENSP00000212015.6:n.1170+61T>A
ENST00000403579.1:c.261+61T>A	ENSP00000384063.1:n.261+61T>A
ENST00000406900.5:c.261+61T>A	ENSP00000384508.1:n.261+61T>A
ENST00000432464.5:c.285+61T>A	ENSP00000409208.1:n.285+61T>A
NM_001142498.1:c.285+61T>A	NP_001135970.1:n.285+61T>A
NM_001314049.1:c.261+61T>A	NP_001300978.1:n.261+61T>A
NM_012238.4:c.1170+61T>A	NP_036370.2:n.1170+61T>A
XM_006717737.2:c.1017+61T>A	XP_006717800.1:n.1017+61T>A
XM_011539561.1:c.594+61T>A	XP_011537863.1:n.594+61T>A
NM_012238.5:c.1170+61T>A MANE Select	NP_036370.2:n.1170+61T>A
NM_001142498.2:c.285+61T>A	NP_001135970.1:n.285+61T>A